A Novel Missense Mutation of Arginine Vasopressin Receptor 2 in a Chinese Family with Congenital Nephrogenic Diabetes Insipidus: X-Chromosome Inactivation in Female CNDI Patients with Heterozygote 814A>G Mutation

标题
A Novel Missense Mutation of Arginine Vasopressin Receptor 2 in a Chinese Family with Congenital Nephrogenic Diabetes Insipidus: X-Chromosome Inactivation in Female CNDI Patients with Heterozygote 814A>G Mutation
作者
关键词
-
出版物
Biomed Research International
Volume 2022, Issue -, Pages 1-7
出版商
Hindawi Limited
发表日期
2022-07-13
DOI
10.1155/2022/7073158

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